Genome-wide linkage analysis to urinary microalbuminuria in a community-based sample: the Framingham Heart Study. Langefeld, C. Heritability of GFR and albuminuria in Caucasians with type 2 diabetes mellitus. Pattaro, C. Genome-wide association studies of albuminuria: towards genetic stratification in diabetes? CUBN is a gene locus for albuminuria. Teumer, A. Genome-wide association studies identify genetic loci associated with albuminuria in diabetes. Diabetes 65 , — Kramer, H. Brown, L. Admixture mapping identifies an Amerindian ancestry locus associated with albuminuria in hispanics in the United States.
Sandholm, N. Genome-wide association study of urinary albumin excretion rate in patients with type 1 diabetes. Diabetologia 57 , — Haas, M. Genetic association of albuminuria with cardiometabolic disease and blood pressure.
Resolving the topological classification of bismuth with topological defects | Science Advances
Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution. Voskarides, K. Malone, A.
Zhang, Y. Estimation of complex effect-size distributions using summary-level statistics from genome-wide association studies across 32 complex traits. Genovese, G. Association of trypanolytic ApoL1 variants with kidney disease in African Americans. Science , — Naik, R. Association of sickle cell trait with chronic kidney disease and albuminuria in African Americans. Peiris, H. Discovering human diabetes-risk gene function with genetics and physiological assays.
Sevilla, L. Kazrin regulates keratinocyte cytoskeletal networks, intercellular junctions and differentiation. Cell Sci. Pers, T. Biological interpretation of genome-wide association studies using predicted gene functions. Denny, J. Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data. Sundin, O. A common locus for late-onset Fuchs corneal dystrophy maps to 18q Afshari, N. Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.
Brantsma, A. Urinary albumin excretion and its relation with C-reactive protein and the metabolic syndrome in the prediction of type 2 diabetes. Diabetes Care 28 , — Wang, T. Low-grade albuminuria and the risks of hypertension and blood pressure progression. Gerstein, H. Albuminuria and risk of cardiovascular events, death, and heart failure in diabetic and nondiabetic individuals. Benner, C. Prospects of fine-mapping trait-associated genomic regions by using summary statistics from genome-wide association studies.
Yang, J. Common SNPs explain a large proportion of the heritability for human height. Wakefield, J. A Bayesian measure of the probability of false discovery in genetic epidemiology studies. Sieber, K. Integrated functional genomic analysis enables annotation of kidney genome-wide association study loci. Ko, Y. Genetic-variation-driven gene-expression changes highlight genes with important functions for kidney disease.
Gillies, C. An eQTL landscape of kidney tissue in human nephrotic syndrome. Kirby, A. Sun, B. Genomic atlas of the human plasma proteome. Nature , 73—79 Using the Drosophila Nephrocyte to model podocyte function and disease.watch
What are you looking for?
Hermle, T. Modeling monogenic human nephrotic syndrome in the Drosophila garland cell nephrocyte. Huber, T. Amsellem, S. Cubilin is essential for albumin reabsorption in the renal proximal tubule.
Meng, X. Blobe, G. Role of transforming growth factor beta in human disease. Fuchsberger, C. GWAtoolbox: an R package for fast quality control and handling of genome-wide association studies meta-analysis data. Bioinformatics 28 , — Willer, C. METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 26 , — Bulik-Sullivan, B.
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
Related Jonathan Auf Null: Band 1 (German Edition)
Copyright 2019 - All Right Reserved